# Stephan Sanders

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/stephan-sanders/

## Facts

| Field | Value |
| --- | --- |
| Citations | 52,985 |
| Field | Autism Spectrum Disorder Research |
| h-index | 85 |
| i10-index | 175 |
| Last Known Institution | Oxfam |
| OpenAlex ID | https://openalex.org/A5049906252 |
| ORCID iD | https://orcid.org/0000-0001-9112-5148 |
| Works | 546 |

## Researcher papers

- [Synaptic, transcriptional and chromatin genes disrupted in autism](https://scholariq.org/papers/synaptic-transcriptional-and-chromatin-genes-disrupted-in-autism/)
- [Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci](https://scholariq.org/papers/insights-into-autism-spectrum-disorder-genomic-architecture-and-biology-from-71/)
- [Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism](https://scholariq.org/papers/multiple-recurrent-de-novo-cnvs-including-duplications-of-the-7q11-23-williams/)
- [Integrative functional genomic analysis of human brain development and neuropsychiatric risks](https://scholariq.org/papers/integrative-functional-genomic-analysis-of-human-brain-development-and/)
- [Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations](https://scholariq.org/papers/whole-exome-sequencing-identifies-recessive-wdr62-mutations-in-severe-brain/)
- [De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability](https://scholariq.org/papers/de-novo-mutations-in-protein-kinase-genes-camk2a-and-camk2b-cause-intellectual/)

## Researcher topics

- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)

## Researcher university

- [Oxfam](https://scholariq.org/institutions/oxfam/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.